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Committee for Medicinal Products for Human Use [ENGLISH]

The committee that is responsible for preparing the Agency's opinions on questions concerning human medicines.


EMAs vetenskapliga kommitté som ansvarar för att ta fram förslag på EU-gemensamma beslut om centralt godkända humanläkemedel, till exempel nya godkännanden eller ändrade indikationer. De formella besluten fattas av EU-kommissionen.


Resources and references

Definitions have been translated into the Swedish language from the following sources:

  1. 1. American Society of Gene and Cell Therapy Glossary
  2. 2. Clinical Trials Information System
  3. 3. EMA Glossary of Regulatory Terms
  4. 4. EMA Medical Terms simplifier
  5. 5. Glossary of Terms used in EU Clinical Trials Register
  6. 6. Glossary of Terms U.S Food and Drug Administration
  7. 7. National Human Genome Research Institute “Talking Glossary of Genomic and Genetic Terms”
  8. 8. The Glossary for Advanced Therapies Regen. Med. Dec 2020 Vol. 15 No. 12 Suppl. 1
  9. 9. Toolkit For Patient Focused Therapy Development Glossary

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